Allele Registry

Canonical Allele Identifier: PA2826059001

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV002706423

ClinVar Variation:

1960323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162580.1:p.Trp36Ser	CA412194233 NM_001169109.2:c.107G>C